Job Description

Summary:

The Clinical Research Coordinator is responsible for managing multiple clinical trials from start-up through close-out in compliance with study protocols, GCP, ICH guidelines, and company SOPs. This role ensures high-quality execution of studies while maintaining patient safety and regulatory standards. This is a full-time, onsite, 3-month contract position with a group in Baton Rouge, LA.

Key Responsibilities:

• Coordinate all aspects of assigned clinical trials, including start-up, recruitment, subject visits, data entry, and close-out.
• Manage study documents, regulatory submissions, protocol training, and vendor communication.
• Monitor patient safety, report adverse events, and implement protocol amendments as needed.
• Ensure timely and accurate data entry, query resolution, and quality documentation practices.
• Collaborate with sponsors, CROs, vendors, and internal teams to maintain study compliance and efficiency.
• Perform limited clinical duties (e.g., phlebotomy, ECGs, lab processing) within scope.

Qualifications:

• Bachelor’s degree + 2 years of relevant life science experience, or equivalent (Associate’s degree + 4 years; High School + 6 years with at least 1 year as a CRC).
• Strong knowledge of medical terminology, GCP/ICH guidelines, and clinical trial processes.
• Excellent organizational, problem-solving, and communication skills with the ability to work independently or as part of a team.
• Proficient with Microsoft Office and clinical data systems; detail-oriented and adaptable in a fast-paced environment.

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